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Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia

Yıl 2015, Cilt: 42 Sayı: 4, - , 08.01.2016
https://doi.org/10.5798/diclemedj.0921.2015.04.0625

Öz

Very long chain fatty acids accumulate in many tissues and organs in the peroxisomal disorders due to defects in fatty acid metabolism. Although the disease may be manifested as severe symptoms causing early death due to hypotonia, poor feeding, respiratory problems, cerebral dysgenesis, liver and kidney dysfunctions, it may be presented as late onset with mild symptoms. We presented a 4 months-old male infant with peroxisomal disorder diagnosed by dysmorphic facial appearance, hypotonia since birth, feeding difficulties, respiratory distress, severe cerebral dysgenesis and increased very long chain fatty acids due to its rarity.

Key words: Peroxisomal disorder, hypotonia, severe cerebral dysgenesis

Kaynakça

  • Barry DS, O’Keeffe GW. Peroxisomes: the neuropathological
  • consequences of peroxisomal dysfunction in the developing brain. Int Biochem Cell Biol 2013;45:2012-2015.
  • Aubourg P, Wanders R. Peroxisomal disorders. Handb Clin
  • Neurol 2013;113:1593-1609.
  • Lee PR, Raymond GV. Child neurology: Zellweger syndrome.
  • Neurology 2013;80:207-210.
  • Abe Y, Honsho M, Nakanishi H, et al. Very-long-chain polyunsaturated fatty acids accumulate in phosphatidylcholine
  • of fibroblasts from patients with Zellweger syndrome and acyl-CoA oxidase1 deficiency. Biochim Biophys Acta 2014;1841:610-619.
  • Lines MA, Jobling R, Brady L, et al. Peroxisomal D-bifunctional
  • protein deficiency: three adults diagnosed by wholeexome sequencing. Neurology 2014;82:963-968.
  • Barkovich AJ, Peck WW. MR of Zellweger syndrome. AJNR Am J Neuroradiol 1997;18:1163-1170.
  • Weller S, Rosewich H, Gärtner J. Cerebral MRI as a valuable
  • diagnostic tool in Zellweger spectrum patients. J Inherit Metab Dis 2008;31:270-280.
Toplam 13 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Bölüm Araştırma Yazıları
Yazarlar

Osman Yeşilbaş Bu kişi benim

Hasan Kıhtır Bu kişi benim

Melike Ersoy Bu kişi benim

Hamd Yıldırım Bu kişi benim

Müge Sungur Bu kişi benim

Esra Şevketoğlu Bu kişi benim

Yayımlanma Tarihi 8 Ocak 2016
Gönderilme Tarihi 8 Ocak 2016
Yayımlandığı Sayı Yıl 2015 Cilt: 42 Sayı: 4

Kaynak Göster

APA Yeşilbaş, O., Kıhtır, H., Ersoy, M., Yıldırım, H., vd. (2016). Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia. Dicle Medical Journal, 42(4). https://doi.org/10.5798/diclemedj.0921.2015.04.0625
AMA Yeşilbaş O, Kıhtır H, Ersoy M, Yıldırım H, Sungur M, Şevketoğlu E. Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia. diclemedj. Ocak 2016;42(4). doi:10.5798/diclemedj.0921.2015.04.0625
Chicago Yeşilbaş, Osman, Hasan Kıhtır, Melike Ersoy, Hamd Yıldırım, Müge Sungur, ve Esra Şevketoğlu. “Peroxisomal Disorder Characterized With Severe Cerebral Dysgenesis and Hypotonia”. Dicle Medical Journal 42, sy. 4 (Ocak 2016). https://doi.org/10.5798/diclemedj.0921.2015.04.0625.
EndNote Yeşilbaş O, Kıhtır H, Ersoy M, Yıldırım H, Sungur M, Şevketoğlu E (01 Ocak 2016) Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia. Dicle Medical Journal 42 4
IEEE O. Yeşilbaş, H. Kıhtır, M. Ersoy, H. Yıldırım, M. Sungur, ve E. Şevketoğlu, “Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia”, diclemedj, c. 42, sy. 4, 2016, doi: 10.5798/diclemedj.0921.2015.04.0625.
ISNAD Yeşilbaş, Osman vd. “Peroxisomal Disorder Characterized With Severe Cerebral Dysgenesis and Hypotonia”. Dicle Medical Journal 42/4 (Ocak 2016). https://doi.org/10.5798/diclemedj.0921.2015.04.0625.
JAMA Yeşilbaş O, Kıhtır H, Ersoy M, Yıldırım H, Sungur M, Şevketoğlu E. Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia. diclemedj. 2016;42. doi:10.5798/diclemedj.0921.2015.04.0625.
MLA Yeşilbaş, Osman vd. “Peroxisomal Disorder Characterized With Severe Cerebral Dysgenesis and Hypotonia”. Dicle Medical Journal, c. 42, sy. 4, 2016, doi:10.5798/diclemedj.0921.2015.04.0625.
Vancouver Yeşilbaş O, Kıhtır H, Ersoy M, Yıldırım H, Sungur M, Şevketoğlu E. Peroxisomal disorder characterized with severe cerebral dysgenesis and hypotonia. diclemedj. 2016;42(4).